Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,479 positions on this site are linked to Height, out of 2,509,486 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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Strength of the evidence: all 2+ 3+ 4 Connections: all only those linked to a condition, drug or sense

← Back to Height

Standard

Height (baseline)

near SCGN · rs115264061

See detailed info → Standard

Height (baseline)

SMG1P7 · rs115130525

See detailed info → Standard

Height

near MATN1 · rs1149036

See detailed info → Standard

Height (baseline)

USP37 · rs114727537

See detailed info → Standard

Height (baseline)

SPSB1 · rs113702200

See detailed info → Standard

Height (baseline)

PPP1R3E · rs113316623

See detailed info → Standard

Height (baseline)

DYSF · rs112901379

See detailed info → Standard

Height (baseline)

near SDR16C6P · rs111909673

See detailed info → Standard

Height (baseline)

ATP6V1G1P6 · rs111706939

See detailed info → Standard

Height (baseline)

HLX-AS1 · rs11118617

See detailed info → Standard

Height (baseline)

MRPS35-DT · rs11049101

See detailed info → Standard

Height (baseline)

MYBPC3 · rs11039186

See detailed info → Standard

Height (baseline)

KIF17 · rs10916849

See detailed info → Standard

Height (standard GWA)

PRKCZ · rs10910029

See detailed info → Standard

Height (baseline)

LNCAROD · rs10824623

See detailed info → Standard

Height

DCDC2 · rs10806987

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Height

TOX · rs1075418

See detailed info → Standard

Height (baseline)

CEP55 · rs10748604

See detailed info → Standard

Sitting height ratio

C10orf90 · rs10736877

See detailed info → Standard

Height (baseline)

near FABP6 · rs10463076

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Questions about variants on this site

What is a "variant" page on this site?

One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.

Where does new variant data come from?

The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.

Does being listed here mean a variant causes a condition?

No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.

Can I search this list by gene or rsID?

Yes — the search box above matches gene symbols and rsIDs as well as trait names.